Evidence map›Paper›PMID 42206098›Full record

ReviewBMJ neurology open2026

Slowing the curve: a single-arm meta-analysis of mFARS outcomes following omaveloxolone treatment in Friedreich ataxia.

Aasim Ali, Waqar Ahmed Cheema, Fiza Nisar, Ufaq Reyaz, Muhammad Saad, Muhammad Talha, Sameen Sarfraz, Ahmad Butt, Muhammad Shamoon, Armaghana Abdullah and 5 more

Abstract readReview
In one paragraph

Review in BMJ neurology open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Aasim AliNeurology Daepartment, Allied Hospital Faisalabad, Faisalabad, Punjab, Pakistan.ORCID https://orcid.org/0009-0001-6002-4325
Waqar Ahmed CheemaInternal Medicine Department, Allied Hospital Faisalabad, Faisalabad, Pakistan.ORCID https://orcid.org/0009-0001-1472-6799
Fiza NisarNeurology Daepartment, Allied Hospital Faisalabad, Faisalabad, Punjab, Pakistan.
Ufaq ReyazInternal Medicine Department, Allied Hospital Faisalabad, Faisalabad, Pakistan.
Muhammad SaadNeurology Daepartment, Allied Hospital Faisalabad, Faisalabad, Punjab, Pakistan.
Muhammad TalhaInternal Medicine Department, Allied Hospital Faisalabad, Faisalabad, Pakistan.
Sameen SarfrazNeurology Daepartment, Allied Hospital Faisalabad, Faisalabad, Punjab, Pakistan.
Ahmad ButtInternal Medicine Department, Allied Hospital Faisalabad, Faisalabad, Pakistan.
Muhammad ShamoonNeurology Daepartment, Allied Hospital Faisalabad, Faisalabad, Punjab, Pakistan.
Armaghana AbdullahInternal Medicine Department, Allied Hospital Faisalabad, Faisalabad, Pakistan.
Muhammad Asad ShabbirInternal Medicine Department, Allied Hospital Faisalabad, Faisalabad, Pakistan.
Muhammad TalhaInternal Medicine Department, Allied Hospital Faisalabad, Faisalabad, Pakistan.
Hammad AzamInternal Medicine Department, Allied Hospital Faisalabad, Faisalabad, Pakistan.
Muhammad AbdullahInternal Medicine Department, Allied Hospital Faisalabad, Faisalabad, Pakistan.
Aimen AnwaarInternal Medicine Department, Allied Hospital Faisalabad, Faisalabad, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Friedreich ataxia (FRDA) is a progressive neurodegenerative disorder with limited treatments. Omaveloxolone, an Nrf2 activator, was approved based on a phase III trial showing modified Friedreich Ataxia Rating Scale (mFARS) improvement. Real-world and long-term data now require synthesis. To perform a single-arm meta-analysis pooling mean change in mFARS from baseline across all published omaveloxolone studies and interpret findings against natural history. Four studies (MOXIe Part 1, Part 2, open-label extension, Italian observational) comprising 248 patients were included. Data were harmonised using standard conversions. A random-effects model was used with subgroup and sensitivity analyses. The pooled mean ΔmFARS was -0.05 (95% CI -2.98 to 2.88; p=0.97). Subgroup analysis showed significant improvement in controlled trials (-2.19; 95% CI -3.12 to -1.27; p<0.00001) and consistent progression in real-world studies (+2.85; 95% CI 1.62 to 4.08; p<0.00001). Sensitivity analyses confirmed robustness. Controlled trials demonstrate significant short-term improvement with omaveloxolone, while real-world data show consistent progression at rates substantially slower than natural history. These complementary findings support a disease-modifying effect of omaveloxolone in FRDA.

Indexed as

CLINICAL NEUROLOGYEVIDENCE-BASED NEUROLOGY

Identifiers

PMID42206098
PMCPMC13202156

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.